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Visible Light-Driven Water Oxidation by a Molecular Ruthenium Catalyst in Homogeneous System

Duan, Lele (författare)
KTH,Organisk kemi
Xu, Yunhua (författare)
KTH,Organisk kemi
Zhang, Pan (författare)
KTH,Molekylär elektronik, CMD
visa fler...
Wang, Mei (författare)
KTH,Molekylär elektronik, CMD
Sun, Licheng (författare)
KTH,Organisk kemi,Molekylär elektronik, CMD
visa färre...
 (creator_code:org_t)
2009-12-08
2010
Engelska.
Ingår i: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 49:1, s. 209-215
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Discovery of an efficient catalyst bearing low overpotential toward water oxidation is a key step for light-driven water splitting into dioxygen and dihydrogen. A mononuclear ruthenium complex, Ru(II)L(pic)(2) (1) (H2L = 2,2'-bipyridine-6,6'-dicarboxylic acids pic = 4-picoline), was found capable of oxidizing water eletrochemically at a relatively low potential and promoting light-driven water oxidation using a three-component system composed of a photosensitizer, sacrificial electron acceptor, and complex 1. The detailed electrochemical properties of 1 were studied, and the onset potentials of the electrochemically catalytic curves in pH 7.0 and pH 1.0 solutions are 1.0 and 1.5 V, respectively. The low catalytic potential of 1 under neutral conditions allows the use of [Ru(bpy)(3)](2+) and even [Ru(dmbpy)(3)](2+) as a photosensitizer for photochemical water oxidation. Two different sacrificial electron acceptors, [Co(NH3)(5)Cl]Cl-2 and Na2S2O8, were used to generate the oxidized state of ruthenium tris(2,2'-bipyridyl) photosensitizers. In addition, a two-hour photolysis of I in a pH TO phosphate buffer did not lead to obvious degradation, indicating the good photostability of our catalyst. However, under conditions of light-driven water oxidation, the catalyst deactivates quickly. In both solution and the solid state under aerobic conditions, complex 1 gradually decomposed via oxidative degradation of its ligands, and two of the decomposed products, sp(3) C-H bond oxidized Ru complexes, were identified. The capability of oxidizing the sp(3) C-H bond implies the presence of a highly oxidizing Ru species, which might also cause the final degradation of the catalyst.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Nyckelord

O-O BOND
ARTIFICIAL PHOTOSYNTHESIS
FUNCTIONAL-MODEL
EXCITED-STATE
RU(II) COMPLEXES
REDOX PROPERTIES
PHOTOSYSTEM-II
O-2 EVOLUTION
OXYGEN
LIGAND
Chemistry
Kemi

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Duan, Lele
Xu, Yunhua
Zhang, Pan
Wang, Mei
Sun, Licheng
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NATURVETENSKAP
NATURVETENSKAP
och Kemi
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Inorganic Chemis ...
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Kungliga Tekniska Högskolan

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